Nneji Lotanna Micah, Adeola Adeniyi Charles, Ayoola Adeola Oluwakemi, Oladipo Segun Olayinka, Wang Yun-Yu, Malann Yoila D, Anyaele Okorie, Nneji Ifeanyi Christopher, Rahman Md Mizanur, Olory Caroline Samuel
State Key Laboratory of Genetic Resources and Evolution, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, 650223, Yunnan, China.
Sino-Africa Joint Research Centre, Chinese Academy of Sciences, Kunming, 650223, Yunnan, China.
Mol Biol Rep. 2020 Dec;47(12):9441-9457. doi: 10.1007/s11033-020-05984-5. Epub 2020 Nov 16.
Accurate identification of species is a prerequisite for successful biodiversity management and further genetic studies. Species identification techniques often require both morphological diagnostics and molecular tools, such as DNA barcoding, for correct identification. In particular, the use of the subunit I of the mitochondrial cytochrome c oxidase (COI) gene for DNA barcoding has proven useful in species identification for insects. However, to date, no studies have been carried out on the DNA barcoding of Nigerian butterflies. We evaluated the utility of DNA barcoding applied for the first time to 735 butterfly specimens from southern Nigeria. In total, 699 DNA barcodes, resulting in a record of 116 species belonging to 57 genera, were generated. Our study sample comprised 807 DNA barcodes based on sequences generated from our current study and 108 others retrieved from BOLD. Different molecular analyses, including genetic distance-based evaluation (Neighbor-Joining, Maximum Likelihood and Bayesian trees) and species delimitation tests (TaxonDNA, Automated Barcode Gap Discovery, General Mixed Yule-Coalescent, and Bayesian Poisson Tree Processes) were performed to accurately identify and delineate species. The genetic distance-based analyses resulted in 163 well-separated clusters consisting of 147 described and 16 unidentified species. Our findings indicate that about 90.20% of the butterfly species were explicitly discriminated using DNA barcodes. Also, our field collections reported the first country records of ten butterfly species-Acraea serena, Amauris cf. dannfelti, Aterica galena extensa, Axione tjoane rubescens, Charaxes galleyanus, Papilio lormieri lormeri, Pentila alba, Precis actia, Precis tugela, and Tagiades flesus. Further, DNA barcodes revealed a high mitochondrial intraspecific divergence of more than 3% in Bicyclus vulgaris vulgaris and Colotis evagore. Furthermore, our result revealed an overall high haplotype (gene) diversity (0.9764), suggesting that DNA barcoding can provide information at a population level for Nigerian butterflies. The present study confirms the efficiency of DNA barcoding for identifying butterflies from Nigeria. To gain a better understanding of regional variation in DNA barcodes of this biogeographically complex area, future work should expand the DNA barcode reference library to include all butterfly species from Nigeria as well as surrounding countries. Also, further studies, involving relevant genetic and eco-morphological datasets, are required to understand processes governing mitochondrial intraspecific divergences reported in some species complexes.
准确识别物种是成功进行生物多样性管理和进一步开展遗传研究的前提条件。物种识别技术通常既需要形态学诊断方法,也需要分子工具,如DNA条形码技术,才能进行正确识别。特别是,线粒体细胞色素c氧化酶(COI)基因的亚基I用于DNA条形码技术已被证明在昆虫物种识别中很有用。然而,迄今为止,尚未对尼日利亚蝴蝶进行DNA条形码研究。我们评估了首次应用于来自尼日利亚南部的735个蝴蝶标本的DNA条形码技术的实用性。总共生成了699个DNA条形码,记录了属于57个属的116个物种。我们的研究样本包括基于当前研究生成的序列的807个DNA条形码以及从BOLD数据库中检索到的另外108个条形码。我们进行了不同的分子分析,包括基于遗传距离的评估(邻接法、最大似然法和贝叶斯树)以及物种界定测试(TaxonDNA、自动条形码间隙发现法、广义混合尤尔-凝聚法和贝叶斯泊松树过程),以准确识别和界定物种。基于遗传距离的分析产生了163个分离良好的聚类,其中包括147个已描述物种和16个未识别物种。我们的研究结果表明,约90.20%的蝴蝶物种通过DNA条形码得到了明确区分。此外,我们的野外采集记录了10种蝴蝶在该国的首次发现——塞雷纳阿克雷亚蝶、近似丹费尔蒂阿玛乌里斯蝶、扩展加莱纳阿特里卡蝶、微红乔阿内阿克西奥蝶、加莱亚努斯翠灰蝶、洛米耶美凤蝶、白边喷点灰蝶、阿克蒂前美眼蛱蝶、图盖拉前美眼蛱蝶和弗勒苏塔吉亚德斯蝶。此外,DNA条形码显示普通双环蝶和埃瓦戈尔珂洛蝶的线粒体内种内差异超过3%。此外,我们的结果显示总体单倍型(基因)多样性较高(0.9764),这表明DNA条形码技术可以为尼日利亚蝴蝶提供种群水平的信息。本研究证实了DNA条形码技术在识别尼日利亚蝴蝶方面的有效性。为了更好地了解这个生物地理复杂地区DNA条形码的区域差异,未来的工作应扩大DNA条形码参考库,纳入尼日利亚以及周边国家的所有蝴蝶物种。此外,还需要进一步开展涉及相关遗传和生态形态数据集的研究,以了解一些物种复合体中报道的线粒体内种内差异的控制过程。